{"id":11498,"date":"2025-07-26T15:57:52","date_gmt":"2025-07-26T13:57:52","guid":{"rendered":"https:\/\/valintermed.com\/?p=11498"},"modified":"2025-07-26T15:57:52","modified_gmt":"2025-07-26T13:57:52","slug":"gidranentsefaliya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/hydranentsefaliya-2\/","title":{"rendered":"Hydranencephaly"},"content":{"rendered":"
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Hydranencephaly is a rare neurological disorder characterized by the absence or significant reduction in the volume of the cerebral hemispheres. The main features of this pathology are the presence of structures that are normally located at the base of the brain, protected by cerebrospinal fluid, and the presence of the brainstem and cerebellum, which remain relatively intact. Hydranencephaly occurs due to a number of causes, including disturbances in embryonic development associated with genetic abnormalities, infections, or the effects of adverse environmental factors. The disease usually leads to pronounced neurological symptoms, which can range from mild mental retardation to profound neurological disorders and physical dependence on others.<\/p>\n

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